Methods and devices for percutaneous and surgical interventions

ABSTRACT

Methods and devices for performing percutaneous and surgical interventions. The devices comprising a tubular portion and retractable mechanism at the distal end of the tubular portion. The retractable mechanism prevents the device from pulling out of an anatomical structure during complex interventions, for example, when switching from an antegrade to a retrograde approach within a blood vessel, enables the use of a single sheath when declotting AV hemodialysis fistulas and can provide occlusion of blood flow during interventions and means of removal of debris or clot from the blood vessel.

The present invention generally relates to methods and devices forperforming percutaneous and surgical interventions. More particularly,the present invention provides improved vascular sheaths and guidecatheters and methods of use.

BACKGROUND OF THE INVENTION

Vascular sheaths and guide catheters are used routinely ininterventional radiology and interventional cardiology. The sheathserves as a conduit from the skin surface to the artery to allowpassages of catheters, guide wires, stents, angioplasty balloons andsimilar instruments through the subcutaneous track without damaging thesurrounding tissues or the blood vessel itself. The sheath is generallycomposed of four main components. The first is the tubular portion,which is the conduit from the skin surface into the blood vessel. Thesecond portion is a hemostatic valve on the skin surface portion of thesheath. The third component is a sidearm tubing with a stopcock thatallows the sheath to be flushed or aspirated with fluid. The fourthcomponent is a tapered dilator that passes through the tubular portionof the sheath to allow a non-traumatic introduction of the sheath intothe blood vessel. Once the sheath is introduced into the blood vessel,the dilator is then removed to allow passages of catheters. Thesesheaths are used in over 99 percent of all vascular cases. The vascularsheaths are generally used by first puncturing the blood vessel with aneedle, followed by insertion of a guide wire. A dilator, having mountedin the vascular sheath, is then advanced into the blood vessel over theguide wire. The dilator is removed, leaving the distal end of thevascular sheath inside the blood vessel.

While these current vascular sheaths and methods are generally suitable,they have many drawbacks.

The designs of current vascular sheaths do not adequately maintain thesheaths steadily in the blood vessel. For example the sheaths can beeasily pulled out of the blood vessel during manipulations of cathetersand other devices within the lumen of the sheath.

Further, when using vascular sheaths to perform surgery on carotidartery stenosis, emboli may form during the course of the procedure.These emboli can flow into the cerebral vasculature, leading to ischemicstroke. Current sheaths do not adequately prevent the flow of emboliinto the cerebral vasculature.

Still further, during a number of vascular procedures, it would beadvantageous to reposition the sheath from a retrograde position(against the blood flow) to an antegrade position (with the blood flow)or visa-versa. For example, when placing a stent in a vessel, performingan angioplasty or performing a thrombectomy, a vascular sheath isinserted to the treatment location using a retrograde common femoralarterial approach. However, during such procedures, it is oftendiscovered that there are a plurality of treatment locations. Forexample, in performing an angioplasty procedure on an obstructed vessel,it is not uncommon to find that the vessel is obstructed at more thanone location. For example, one location may be located upstream from theinsertion point of the vascular sheath and another location may belocated downstream from the insertion point of the vascular sheath.Thus, it would be very desirable to be able to position the vascularsheath in a retrograde position to treat the first location, followed byrepositioning of the vascular sheath in an antegrade position to treatthe second location. This is extremely difficult to do with the currentsheath technology. These sheaths pull out of the vessel when theoperator tries to redirect the sheath, and the operator loses vascularaccess. Thus, with current sheath designs, the first location is firsttreated by making an incision to provide retrograde access to the firstobstructed location. After the first location is treated, the sheath isremoved and the puncture in the vessel must be allowed to heal prior totreatment of the second obstructed location. It can take as long as aweek for the puncture in the vessel to heal. The patient must thenreturn for a second procedure to treat the second obstructed location,which requires a second incision.

Additionally, current methods for Fogarty balloon thrombectomy require asurgical incision of the blood vessel and clamping of the blood vesseldistal to the incision (for an iliac artery thrombectomy). The balloonis passed to the superior most aspect of the clot, inflated and pulledinferiorly, dragging the clot to the arteriotomy site and out of theblood vessel. If the same aforementioned procedure were performedpercutaneous with current sheath technology, the size mis-match betweenthe blood vessel and the sheath would cause the clot to flow past thesheath and into the distal blood vessels.

Thus, any improvements in vascular sheaths would be desirable.

SUMMARY OF THE INVENTION

The present invention provides improved devices for performingpercutaneous and surgical interventions, particularly vascular sheathsand guide catheters, and methods of use thereof. More particularly, thepresent invention provides a device that may be manipulated within ananatomical structure while eliminating the possibility of the devicelosing access to the anatomical structure during such manipulation.

For example, in one embodiment, the device comprises a vascular sheathor a guide catheter that may be inserted and repositioned within a bloodvessel while eliminating the possibility of losing vascular accessduring such manipulation. In one embodiment, the vascular sheath orguide catheter may be repositioned from a retrograde to an antegradeposition in a blood vessel, and vice versa, while eliminating thepossibility of losing vascular access during such manipulation.

The devices of the present invention can be used during all types ofpercutaneous interventions and surgical interventions including, forexample, vascular percutaneous interventions such as thrombectomies,carotid stenting, hemodialysis AV fistula declotting, superficialfemoral artery interventions, pelvic vasculature stenting, and biliaryinterventions and kidney stone extraction.

In an exemplary embodiment, the device includes a tubular portion havinga proximal end and a distal end. During use, at least a portion of thedevice is inserted into an anatomical structure distal end first.Located near the distal end of the tubular portion is a mechanism thatprevents the device from losing access to the anatomical structureduring manipulation of the device. At least one lumen further extendsalong the length of the tubular portion from the proximal end to thedistal end. The lumen is designed so that materials can be removed fromand added to the anatomical structure through the lumen. For example,emboli, blood clots and other materials can be evacuated from a bloodvessel using an aspiration technique or by pulling clot or othermaterial out through the sheath by means of a Fogarty balloon, andagents, such as medicaments, anticoagulants and contrast media may beinjected into the blood vessel. In embodiments wherein the device is avascular sheath, the lumen is sized so that various instruments may beinserted through the sheath to the treatment site. In embodimentswherein the device is a guide catheter, the lumen is also sized so thatvarious instruments may be inserted through the sheath to the treatmentsite.

In some embodiments, for example, wherein the device is a vascularsheath, a hemostatic valve is located at the proximal end of the tubularportion. In some embodiments, the hemostatic valve is removable. A sidearm in fluid communication with the lumen can further be located nearthe proximal end of the tubular portion to allow emboli, blood clots andother materials to be evacuated from the blood vessel through thetubular portion and to allow agents, such as medicaments, anticoagulantsand contrast media to be injected into the blood vessel through thetubular portion. In some embodiments, a tapered dilator further passesfrom the distal end to the proximal end through the tubular portion. Indevices used for balloon thrombectomy, a silicon pinch valve wouldfurther be included near the proximal end of the tubular portion.

The mechanism that prevents the device from losing access to theanatomical structure during manipulation of the device can vary.

In one embodiment, the mechanism is an inflatable balloon located at ornear the distal end of the tubular portion. The inflatable balloon canbe designed to inflate to a variety of shapes and sizes. For example, inone embodiment, the inflatable balloon inflates to an overall round oroval shape and is situated coaxial with the tubular portion. In anotherembodiment, the inflatable balloon inflates to a funnel-like shapecoaxial with the tubular portion, wherein the smaller cross-section ofthe funnel-like shaped balloon is towards the proximal end of thetubular portion and the larger cross-section of the funnel-like shapedballoon is towards the distal end of the tubular portion. In yet anotherembodiment, a plurality of inflatable balloons are positioned to inflateabout the outer circumference of the tubular portion.

In embodiments wherein the mechanism is in the form of one or moreinflatable balloons, one or more inflation ports are further locatednear the proximal end of the tubular portion for inflation of the one ormore balloons. The one or more inflation ports are in communication withthe one or more balloons via, for example, one or more inflationchannels extending from the inflation port(s) to the balloon(s) throughthe wall of the tubular portion.

In another embodiment, the mechanism comprises one or more retractableextensions near the distal end of the tubular portion. For example, twoor more retractable arm-like extensions may be located near the distalend of the tubular portion. These retractable extensions are remotelydeployed and retracted by a user of the device with adeployment/retraction mechanism located near the proximal end of thedevice. During insertion of the device into the anatomical structure,these extensions would be retracted (e.g. housed within the tubularportion or folded back against the side surfaces of the tubular portion)such that the cross section of the tubular portion is not significantlyincreased during insertion of the device. As used herein, no“significant” increase in the cross-section of the tubular portion meansthat the mechanism does not overdilate the arteriotomy (the incision inthe anatomical structure through which the device is inserted). Uponinsertion of the device into the anatomical structure to the desiredsite, the extensions could then be deployed.

The device of the present invention provides a number of advantages overprior devices. For example, by forming the device with a mechanism, suchas a balloon or one or more extensions, at the distal end of the tubularportion, the mechanism prevents the device from pulling out of aanatomical structure during complex interventions, for example, whenswitching from a retrograde to an antegrade approach within a bloodvessel (i.e. from a position pointing towards the head to a positionpointing towards the feet) and vice versa.

Use of balloon or extension mechanisms further enables the use of asingle device when declotting AV hemodialysis fistulas.

The device of the present invention also serves as a protection deviceduring any number of procedures. For example, during use of the devicein a blood vessel, the mechanism on the distal end of the device can bedeployed to provide occlusion of antegrade blood flow duringinterventions and protect against embolization. For example, during theplacement of an internal carotid artery stent, using current vascularsheaths, the antegrade blood flow can cause embolic material topropagate into the intracerebral circulation, thereby causing a stroke.By inflating the one or more balloons in the carotid artery inaccordance with the present invention, or, for example, by deploying oneor more extensions that occlude the blood vessel, antegrade flow can beprevented. Retrograde flow would be provided from the contralateralcarotid artery. Similarly, during percutaneous coronary interventions ineither native vessels or bypass grafts, inflation of the balloon servesas a protection device, preventing distal emboli from propagatingforward. In addition, during a suction thrombectomy, if a clot haslodged in a blood vessel, antegrade flow will apply a pressure head tokeep the clot lodged in its position. By occluding the lumen with theballoon or extension mechanisms on the sheath, back-bleeding causes theclot to propagate towards the vascular sheath, and the clot can beaspirated through the vascular sheath or pulled through the vascularsheath using a Fogarty balloon. Still further, the balloon or extensionmechanisms can also prevent blood flow from passing through the bloodvessel, which is advantageous during thrombectomy to prevent embolicmaterial from propagating downstream.

During each of these procedures, after occlusion of the vessel, theembolic material, clot or other materials in the blood vessel could thenbe aspirated through the vascular sheath or pulled through the vascularsheath using a Fogarty balloon.

Alternatively, during each of these procedures, after occlusion of thevessel, a continuous flow reversal could be created. For example, acontinuous flow reversal could be created by forming a circuit from theblood vessel, through the distal end of the tubular portion, through thetubular portion, and into a target vessel. This would require vascularaccess to the target vessel. Such continuous flow reversal would beuseful, for example, in performing a procedure wherein materials, forexample emboli, blood clots, or blood, are transferred from a donorblood vessel into a recipient blood vessel. For example, the devicecould be used to occlude a donor vessel and prevent emboli, blood clotsand other materials from propagating into the coronary vasculature,followed by transfer of the emboli, blood clots and other materials to arecipient blood vessel wherein the danger of having the materialspropagate into the coronary vasculature is eliminated. In thisembodiment, the vascular sheath would be inserted in the donor bloodvessel and, a continuous flow reversal could be created by forming acircuit between the “donor” vessel housing the embolic material to a“recipient” vessel elsewhere in the body. The circuit, thus, wouldextend from the distal portion of the tubular portion, through thetubular portion, and into a recipient vessel. Vascular access to therecipient vessel could be provided, for example, by a tube, a guidecatheter or a vascular sheath. Thus, for example, a vascular sheath inaccordance with the present invention could be inserted in the donorvessel, and the side-arm of the vascular sheath could be connected tothe recipient vessel, for example, via tubing or via a second vascularsheath or a guide catheter. In some embodiments, a pumping mechanism isinterposed in the circuit between the donor and recipient vessels toassist in reversing the blood flow.

Preferably, during the continuous flow reversal procedure, the balloonor extensions could be retracted or partially retracted at any point inthe procedure to allow reperfusion of blood flow through the bloodvessel.

Continuous flow reversal could also be useful in a procedure whereinblood is transferred from one patient to another, or from one site in apatient to another site in the same patient either during cardiac bypasssurgery or during carotid artery surgery. In such procedures, the deviceof the present invention, for example, in the form of a vascular sheathor guide catheter, would be inserted into a donor vessel. The device ofthe present invention would then be connected to a recipient vessel via,for example, a tube, conventional guide catheter, conventional vascularsheath, or second device in accordance with the present invention. Thedevice of the present invention would be particularly helpful onpreventing the loss of vascular access during the blood transferprocedure.

Methods in accordance with the present invention comprise making a smallincision in the upper thigh or other insertion site to provide access tothe target location. The device of the present invention is theninserted into the anatomical structure. For example, when the anatomicalstructure is a blood vessel, a needle is introduced through the incisioninto the blood vessel. A guide wire is then inserted through the needleinto the blood vessel using a retrograde approach. The device is theninserted over the guide wire and is passed into the blood vessel to adesired depth using a retrograde approach. In embodiments wherein thedevice is guide catheter, a vascular sheath is typically first insertedand the guide catheter is inserted through the vascular sheath. Inembodiments wherein the device is a vascular sheath, the vascular sheathwith dilator in the central lumen is inserted over the guide wire and ispassed into the blood vessel to a desired depth using a retrogradeapproach. The guide wire and dilator are removed and the vascular sheathremains positioned in the blood vessel. Once the device is positionedwithin the anatomical structure, the mechanism is then activated, e.g.by inflating the balloon(s) at the distal end of the tubular portionthrough the inflation port or deployment of the extension(s). If aprocedure requiring the blood vessel to be occluded is being performed,the one or more balloons are inflated until the vessel is completelyoccluded. Further, the one or more extensions can be designed such thatthe vessel can be completely occluded by the extensions, by, forexample, forming the one or more extensions to extend outwards from thetubular portion in a circle arrangement or a funnel-like arrangement.

To aspirate emboli, blood clots and other materials from a blood vessel,an aspiration device is connected to the device, for example, anaspiration device may be connected to the vascular sheath through theside-arm, and the material(s) aspirated from the blood vessel, throughthe tubular portion and out of the device. If agents are to be injectedinto the anatomical structure, e.g. a blood vessel, a syringe or similarinjection mechanism is connected to the device, for example, to theside-arm of a vascular sheath, and the agent is injected through thedevice into the anatomical structure. In embodiments wherein the deviceis a vascular sheath, various devices such as, for example, catheters,guide wires, stents, angioplasty balloons and similar instruments canalso be inserted through the tubular portion for various procedures.

If the surgeon wishes to reposition the device to an antegrade positionso that the surgeon can, for example, perform a thrombectomy on theother side of the puncture site into the blood vessel, the surgeoninflates or deflates the balloon(s) such that the cross-section of thetubular portion plus balloon(s) is smaller than the diameter of theblood vessel and larger than the arteriotomy (the incision in the bloodvessel through which the device was inserted) and simply pulls thedevice back towards the insertion point. The device is then pulledoutwards through the incision, but not completely out of the incision.Then, the device is manipulated and pushed back into the blood vessel inan antegrade position. The device can, likewise, be repositioned from anantegrade to a retrograde position. In the embodiment where themechanism comprises one or more extensions, the surgeon, likewise,deploys the extension(s) such that the cross-section of the tubularportion of the device plus extension(s) is smaller than the diameter ofthe blood vessel and larger than the arteriotomy (the incision in theblood vessel through which the vascular sheath was inserted) and simplypulls the device back towards the insertion point. The device is thenpulled outwards through the incision, but not completely out of theincision. Then, the device is manipulated and pushed back into the bloodvessel in an antegrade position, possibly over a guide wire with thedilator in the central lumen of the device. The sheath can, likewise, berepositioned from an antegrade to a retrograde position. In the aboveprocedures, the balloon(s) or extension(s) prevent the device from beingcompletely withdrawn from the blood vessel, so that the operator canmanipulate the device without the concern of losing vascular access.

Methods of the invention also include use of the device to provideocclusion of antegrade blood flow during interventions and protectagainst embolization.

For example, in one embodiment, the device is inserted into the bloodvessel and the mechanism (i.e. balloon(s) or extension(s)) is deployeduntil the vessel is occluded and antegrade blood flow is prevented. Aninternal carotid artery, coronary artery, or renal artery stent can thenbe placed within the vessel. By preventing antegrade blood flow, themechanism will prevent embolic material from propagating into theintracerebral circulation.

In another embodiment, during percutaneous coronary interventions ineither native vessels or bypass grafts, deployment of the mechanism(i.e. balloon(s) or extension(s)) to occlude the vessel functions toprevent distal emboli from propagating forward.

In another embodiment, during a suction thrombectomy, the mechanism(i.e. balloon(s) or extension(s)) is deployed to occlude the vessel,thereby causing back-bleeding. The back-bleeding will then cause anyclots lodged in the blood vessel to propagate towards the device. Theclot can then be removed by aspirating it through the device or pullingit through the device using a Fogarty balloon.

In yet another embodiment, the mechanism (i.e. balloon(s) orextension(s)) can be deployed during a thrombectomy to prevent bloodflow from passing through the blood vessel and around the device, which,in turn, prevents embolic material from propagating downstream.

In yet another embodiment, the device of the present invention could beused to create continuous flow reversal. For example, the device of thepresent invention is inserted in a target blood vessel and is alsoconnected to a recipient blood vessel, such that materials could betransferred from the target blood vessel into the recipient bloodvessel. In this embodiment, vascular access to the recipient vesselwould be required. For example, the device of the present inventioncould be connected to tubing, to a conventional guide catheter, to aconventional vascular sheath, or to a second device in accordance withthe present invention, which, in turn is inserted in the recipient bloodvessel. The continuous flow reversal could then be used to transfermaterials, such as clots and embolic materials, from a target vesselwhere there is a risk that the materials will propagate to the coronaryor cerebral vasculature to a recipient vessel wherein this risk iseliminated. The continuous flow reversal could also be used to simplytransfer blood from a target vessel to a recipient vessel, for example,in performing a blood transfer from one patient to another.

During the continuous flow reversal, the mechanism may be deployed toocclude the vessel, for example, if there is a risk that clots andembolic material may propagate to the cerebral vasculature.Alternatively, the mechanism may be deployed not to occlude the vessel,but, rather, to maintain vascular access if, for example, there isminimal risk that clots and embolic material may propagate to thecerebral vasculature. If the mechanism is deployed to occlude thevessel, the method of continuous flow reversal may further includereperfusion of blood. For example, if reestablishment of the flow ofblood to the heart is desired for a period of time during the procedure,the mechanism may be retracted during the procedure so that the vesselis no longer occluded and blood flow is reestablished. After perfusionof the blood is reestablished for a desired period of time, themechanism may again be deployed to occlude the vessel. In someembodiments, during reperfusion, the circuit between the target bloodvessel and recipient blood vessel can be blocked so that reperfusion iscarried out while transfer of materials from the donor to recipientblood vessel is stopped. Then, after perfusion of the blood isreestablished for a desired period of time, the circuit may then beopened to continue transfer of materials from the donor to recipientblood vessel. During this time, the vessel may remain not occluded ormay again be occluded by redeployment of the mechanism.

Other aspects and embodiments of the invention are discussed infra.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a side view of a device for performing percutaneous andsurgical interventions with a deflated balloon mechanism in accordancewith one embodiment of the present invention.

FIG. 2 shows a side view of the device shown in FIG. 1, having aninflated circular shaped balloon in accordance with one embodiment ofthe present invention.

FIG. 3 shows a side view of the device shown in FIG. 1, having aninflated cone or funnel shaped balloon in accordance with anotherembodiment of the present invention.

FIG. 4 shows a side view of a device for performing percutaneous andsurgical interventions having a catheter hub at its proximal end and adeflated balloon mechanism in accordance with one embodiment of thepresent invention.

FIG. 5 shows a side view of the device in FIG. 4, having an inflatedcone or funnel shaped balloon in accordance with one embodiment of thepresent invention.

FIG. 6 shows a side view of a device for performing percutaneous andsurgical interventions having a catheter hub at its proximal end and aninflated balloon mechanism flush with the distal end of the tubularportion in accordance with one embodiment of the present invention.

FIG. 7 shows a front view of a device for performing percutaneous andsurgical interventions having an inflated balloon and a single ballooninflation aperture in accordance with one embodiment of the presentinvention.

FIG. 8 shows a front view of a device for performing percutaneous andsurgical interventions having an inflated balloon and an open circularstrip for balloon inflation in accordance with another embodiment of thepresent invention.

FIG. 9 shows a side view of the device of FIG. 7 showing a singleballoon inflation channel and aperture.

FIG. 10 shows a side view of a device for performing percutaneous andsurgical interventions having an inflated balloon, a single ballooninflation channel and a plurality of balloon inflation apertures.

FIG. 11 shows a shows a side view of a device for performingpercutaneous and surgical interventions having an inflated balloon, aplurality of balloon inflation channels and a plurality of ballooninflation apertures.

FIG. 12 shows a shows a side view of a device for performingpercutaneous and surgical interventions having a plurality of inflatableballoons near the distal end of the tubular portion.

FIG. 13 shows a shows a side view of a device for performingpercutaneous and surgical interventions having a plurality of inflatableballoons near the distal end of the tubular portion and a single ballooninflation channel that splits to provide inflation to each of theballoons.

FIG. 14 shows a shows a side view of a device for performingpercutaneous and surgical interventions having a plurality of inflatableballoons near the distal end of the tubular portion and a single ballooninflation channel that extends to a ring that provides inflation to eachof the balloons.

FIG. 15 shows a side view of a device for performing percutaneous andsurgical interventions having a plurality of deployable extensionsextending from the distal end of the device in accordance with oneembodiment of the present invention.

FIG. 16 shows a side view of the distal end of a device for performingpercutaneous and surgical interventions having a plurality of extensionsextending in a funnel-like shape from the distal end of the device inaccordance with one embodiment of the present invention.

FIG. 17 shows a side view of the distal end of a device for performingpercutaneous and surgical interventions having a plurality ofextensions, with a material connecting the extensions together,extending in a funnel-like shape from the distal end of the device inaccordance with another embodiment of the present invention.

FIG. 18 shows a side view of the distal end of a device for performingpercutaneous and surgical interventions having a plurality of extensionsextending in a circular-like shape from the distal end of the device inaccordance with one embodiment of the present invention.

FIG. 19 a-b show a shows a side view of a device for performingpercutaneous and surgical interventions having a tapered distal end intowhich one or more mechanisms are retracted (19 a) and deployed (19 b) inaccordance with one embodiment of the present invention.

FIG. 20 a-b show a side view of a device for performing percutaneous andsurgical interventions having a tapered section along its length endinto which one or more mechanisms are retracted (20 a) and deployed (20b) in accordance with one embodiment of the present invention.

FIG. 21 shows a side view of the device shown in FIG. 1, having aninflated U-like shaped balloon in accordance with one embodiment of thepresent invention.

FIG. 22 shows an exploded view of a silicone pinch valve assembly.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides methods and devices for performingpercutaneous and surgical interventions. The device includes a mechanismnear its distal end that prevents the device from pulling out of ananatomical structure, for example, a blood vessel during complexinterventions.

In one preferred embodiment, the device is designed for performing avariety of vascular percutaneous interventions. For example, in onepreferred embodiment, the device is in the form of a vascular sheath ora guide catheter and the mechanism near its distal end prevents thevascular sheath of guide catheter from pulling out of a blood vessel,for example, when switching from a retrograde to an antegrade approachand vice versa. The mechanism also allows the operator to use a singlesheath when declotting AV hemodialysis fistulas. Further, the mechanismcan serve as a lumen occluder while allowing large interventionaldevices to be passed through the sheath. This property, an embolicprotection device, is particularly helpful during thrombectomy andvascular interventions.

Referring now to the various figures of the drawing, wherein likereference characters refer to like parts, there is shown various viewsof a device for performing percutaneous and surgical interventions 1, inaccordance with the invention. The device is shown in the Figures andwill be described below with particular reference to vascular sheaths.However, it is to be understood that the device is not limited tovascular sheaths and may include any type of devices for use inperforming percutaneous and surgical interventions. For example, thedevice may also be in the form of a guide catheter. Devices forperforming percutaneous and surgical interventions, including vascularsheaths and guide catheters, are well-known and, thus, althoughdescribed and shown with reference to a preferred embodiment, thegeneral features (e.g. size, shape, materials) of the a device forperforming percutaneous and surgical interventions 1 may be inaccordance with conventional devices for performing percutaneous andsurgical interventions.

As shown in FIGS. 1-3, one embodiment of the vascular sheath 1 includesa tubular portion 2 having a proximal end 4 and a distal end 6. A lumen3 extends from the proximal end 4 to the distal end 6 of the tubularportion 2. A hemostatic valve 8 is located at the proximal end 4 of thetubular portion 2 to prevent leakage of blood out of the sheath. Aside-arm 14 in fluid communication with the lumen 3 may also be locatednear the proximal end 4 of the tubular portion 2.

Guide catheters are similar in general structure to vascular sheaths buttypically do not include a hemostatic valve or a side arm. Further,guide catheters are not typically used in with a dilator. Generally,guide catheters are used in combination with vascular sheaths and areinserted through the lumen of a vascular sheath. Guide catheters arepredominantly used in coronary interventions and can have a variety ofshapes. Guide catheters are well known and, thus, the general features(e.g. size, shape, materials) of the vascular sheath 1 in the form of aguide catheter may be in accordance with conventional guide catheters.However, in some embodiments of the present invention, it may bedesirable to provide a guide catheter having a hemostatic valve, sidearm, and/or dilator and any combination of these additional elements.

As shown in the Figures, the tubular portion 2 of a device forperforming percutaneous and surgical interventions has a generallycylindrical outer surface 18 and a longitudinal axis 20. The dimensionsof the tubular portion 2 are not particularly limited and can varydepending on the ultimate use of the device. For example, when thedevice is a vascular sheath, in general, the tubular portion is sizedsuch that it properly fits inside a desired blood vessel and providesaccess from the point of insertion to the area being treated. Further,when the vascular sheath is used as a conduit from the skin surface tothe blood vessel to allow passages of catheters, guide wires, andinstruments through vascular sheath 1, the tubular portion 2 is sized toallow these various instruments to be passed through the lumen 3.

Various instruments that are typically passed through the lumen 3 of thetubular portion 2 of a vascular sheath have a maximum diameter rangingfrom about 0.5 mm to about 10 mm and, thus, when the device is avascular sheath used for passing various instruments through the tubularportion 2, the lumen 3 has a diameter of at least about 0.5 mm and,preferably, between about 1.35 mm and about 11 mm.

The outer diameter of the tubular portion 2 is not particularly limitedand may be in accordance with tubular portions of conventional devicefor performing percutaneous and surgical interventions. Generally, theouter diameter of the tubular portion 2 of the device is limited only bythe size of the anatomical structure that it is to be inserted in. Thesize of the tubular portion 2 of the device may also be limited based onthe desired size of the incision through which the device is insertedand which must subsequently be sealed. For example, when the device is avascular sheath, because the vascular sheath can be used on any bloodvessels, the outer diameter can vary depending on the targeted bloodvessel. In general, the tubular portion 2 preferably has an outerdiameter that is smaller than the inner diameter of the blood vessel.The largest blood vessel(s) of the human body is the aorta, which has adiameter ranging from about 20 mm to about 70 mm. Thus, the largestouter diameter of the tubular portion 2 is preferably no greater thanabout 70 mm, preferably, no greater than about 10 mm, and morepreferably, no greater than about 4.5 mm. The smallest blood vessel(s)of the human body are the coronary arteries, infrapopliteal arteries andintra-cranial arteries, which have a diameter ranging from about 1 mm toabout 5 mm. Thus, for use on these small blood vessels, the outerdiameter of the tubular portion 2 is preferably no greater than about 5mm, more preferably, no greater than about 3 mm and, more preferably, nogreater than about 1 mm. In general practice, it is preferable that theouter diameter of the tubular portion 2 is no greater than about 80% ofthe inner diameter of the blood vessel, more preferably, no greater thanabout 20%. However, while it is preferred that the outer diameter of thetubular portion 2 is no greater than the diameter of the blood vesselinto which it is inserted, this is not necessary and, in some cases, theouter diameter of the tubular portion 2 is greater than the diameter ofthe blood vessel into which it is inserted.

In some embodiments, the diameter of the tubular portion 2 narrows at ornear the distal end 6 along the mechanism that prevents the device frompulling out of the anatomical structure. Preferably, in this embodiment,the diameter of the tubular portion 2 at the distal end 6 along themechanism that prevents the device from pulling out of the anatomicalstructure narrows such that the total diameter of the tubular portion 2plus the mechanism in its non-deployed state is equal to or no greaterthan the greatest diameter of the tubular portion along the remainder ofits length. This would ensure that when the device is placed into theanatomical structure, the mechanism would not overdilate thearteriotomy. Thus, for example, in one embodiment, wherein the mechanismis one or more balloons 10, the tubular portion 2 along the one or moredeflated balloons 10 narrows such that the one or more balloons 10 canbe deflated and compressed about the tubular portion 3 to form a totaldiameter of the tubular portion 2 plus deflated balloon(s) 10 that isequal to or no greater than the greatest diameter of the tubular portion2 along the remainder of its length. Further, when the mechanism is oneor more extensions 11, the extensions 11 can be retracted within thetubular portion 2 or can extend along the sides of the tubular portion 2along the narrowed portion such that the total diameter of the tubularportion 2 plus retracted extensions 11 is equal to or no greater thanthe greatest diameter of the tubular portion 2 along the remainder ofits length Thus, for example, if the mechanism is located at the distalend 6 of the tubular portion 2, the tubular portion 2 may taper towardthe distal end as shown in FIG. 19 a-b. If the mechanism is locatedsomewhere between the proximal end 4 and the distal end 6 of the tubularportion 2, the tubular portion 2 may narrow at the location of themechanism, for example, in an hour-glass-like shape as shown in FIG. 20a-b.

The length of the tubular portion 2 is not particularly limited and maybe in accordance with tubular portions of conventional devices forperforming percutaneous and surgical interventions. Generally, thelengths of the tubular portions may vary depending on the use of thedevice, the insertion point of the tubular portion and the distance tothe target area in the anatomical structure. Further, when the device isused as a conduit through which other interventional devices may bepassed, it is often desirable to form the tubular portion 2 so that itis long enough to fully accommodate the longest interventional devicethat will be inserted. For example, in one embodiment the device is avascular sheath 1 designed for use in a variety of cardiac procedures,including procedures within the coronary arteries. The vascular sheath1, when used during cardiac procedures, can be inserted through a bloodvessel in the upper thigh or, alternatively, can be inserted through ablood vessel in the arm. For example, in one preferred embodiment, thevascular sheath 1 is inserted by anesthetizing an area the patient'supper thigh and inserting the vascular sheath 1 through a blood vesselin the upper thigh and towards the heart. As such, the vascular sheath 1preferably has a length ranging from about 5 cm to about 100 cm, morepreferably, from about 5 cm to about 30 cm. The longest interventionaldevices typically have a length that ranges from about 30 cm to about135 cm and, thus, such lengths of tubular portions 2 will accommodate avariety of interventional devices. Of course, the length of the vascularsheath 2 may vary depending on the point of insertion, the distance fromthe point of insertion to the target site and the types ofinterventional devices that will be used in each procedure.

In some embodiments, as shown in FIG. 2, the tubular portion 2 includesindicia 24 along its length to indicate the depth of insertion of thetubular portion 2.

Materials for fabricating the tubular portion 2 of the devices forperforming percutaneous and surgical interventions are well-known andinclude, by way of example TEFLON, polyethylenes, polyamide elastomers,polyurethanes, nylons including polyamide homopolymers and polyamidecopolymers. Because the tubular portion 2 enters the body and anatomicalstructures, the materials used in fabricating the tubular portion 2 arebiocompatible. Preferably, the tubular portion 2 is somewhat flexiblealong its length to allow bending and maneuvering of the tubular portion2 as it passes within an anatomical structure, such as a blood vessel.In addition, the tubular portion 2 preferably is sufficiently stiff toresist kinking, which could damage interventional devices and stentspassed through the lumen 3 of the tubular portion 2. Preferably, atleast the distal end 6 of the tubular portion has adequate rigidity toallow puncture and entry through the wall of an anatomical structure.The tubular portion 2 may be designed with a rigid distal end 6 andflexibility along its length by, for example, fabricating the distal end6 of the tubular portion 2 of a material more rigid than the materialused to form the length of the tubular portion 2. Such materials may bereadily determined by one of skill in the art. Alternatively, the entiretubular portion 2, including the distal end 6, may be fabricated of thesame somewhat flexible material and the walls of the tubular portion 2may be formed thicker at the distal end 6 or, for example, the walls ofthe distal end 6 may be reinforced. In some embodiments, the distal end6 is pointed or beveled to enhance puncturing ability of the tubularportion 2.

A silicone pinch valve 40, shown in FIG. 22, may further be included insome embodiments of the present invention. As shown, the silicone pinchvalve 40 is preferably located near the proximal end 4 of the tubularportion 2, preferably at the proximal end 4 of the tubular portion 2. Insome embodiments, the silicone pinch valve 40 replaces the hemostaticvalve 8 at the proximal end 4 of the tubular portion 2. Thus, thevascular sheath 1 may include a removable hemostatic valve 8 that can beremoved and replaced with the silicone pinch valve 40 if desired. Thesilicone pinch valve 40 could be removably mountable on the tubularportion 2 using, for example, mating threaded portions on the siliconepinch valve 40 and the tubular portion 2. The silicone pinch valve 40may also be designed to snap onto and off of the end of the tubularportion 2. The silicone pinch valve 40 assists in controllingbackbleeding while the vascular sheath 1 is inserted and duringmanipulation of the vascular sheath 1. The silicone pinch valve 40preferably includes a cap 42, preferably fabricated of a plastic, thatfunctions, like a side arm, allowing aspiration and injection ofmaterials through the tubular portion 2. In some embodiments, theplastic cap 42 could be replaced with a side arm. The silicone pinchvalve 40 may also include a Rutner adapter 44 and a silicone septum 46,which function as a hemostatic valve. The Rutner adapter 44 ispreferably rigid and fits into the soft silicone pinch valve 40. Thesilicone septum 46 fits on the end of the Rutner adapter 44. In someembodiments, a central hole (not shown) is located in the siliconeseptum 46 through which small catheters may be introduced. Inembodiments where a large device is introduced through the tubularportion or clot removed from a blood vessel, the silicone septum ispreferably opened or removed to provide a large aperature that is atleast as large as the diameter of the Rutner adapter 44 and lumen 3.

In some embodiments, the silicone pinch valve 40 is positioned betweenthe hemostatic valve 8 and the tubular portion 2. In this embodiment,the hemostatic valve 8 may be directly connected to the silicone pinchvalve 40 or, for example, indirectly connected to the silicone pinchvalve 40. For example, the silicone pinch valve 40 could be locatedinterposed with portions of tubular portion 2 on either side and thehemostatic valve 8 at the proximal end. The hemostatic valve 8 may ormay not be removable or could be of the configuration of the Rutneradapter 44 and silicone septum 46.

Located near the distal end 4 of the tubular portion 2 is a mechanismthat prevents the device 1 from pulling out of an anatomical structureduring complex interventions. Of course, the location of the mechanismis not particularly limited and may also be located elsewhere along thelength of the tubular portion 2. For example, in one embodiment, thedevice is a vascular sheath or a guide catheter and the mechanismprevents the vascular sheath or guide catheter from pulling out of ablood vessel when switching from an antegrade to a retrograde approachand vice versa.

In one embodiment, as shown in FIGS. 1-5, the mechanism is in the formof an inflatable balloon 10 located at the distal end 6 of the tubularportion 2. The inflated balloon 10 is preferably coaxial with thelongitudinal axis 20 of the tubular portion 2. The balloon 10 can befabricated of any expandable or non-expandable materials that arebiocompatible. Preferably, the balloon 10 is fabricated of a materialthat expands away from the tubular portion 2 when inflated such that thedistal end 6 of the tubular portion 2 becomes larger in cross section onaccount of the inflated balloon 10. Preferably, the balloon 10 isfabricated of a material that compresses about the tubular portion 2when deflated such that the balloon 10, when deflated, does notsignificantly increase the diameter of the distal end 6 of the tubularportion 2 when the sheath is inserted and withdrawn. When used herein,“does not significantly increase the diameter of the tubular portion”means that, when the device is placed into the anatomical structure, themechanism would not overdilate the arteriotomy.

Suitable materials for use in forming the balloon 10 are well known inthe art and include, by way of example, PET, polyurethane, polyolefin,polyvinylchloride, any materials used to form angioplasty type balloons,and materials used in forming balloons used in the Swan Ganz catheter orthe Fogarty balloon catheter.

As shown, the balloon 10 is preferably attached directly to the distalend 6 of the tubular portion 2. Of course, the balloon 10 may also belocated elsewhere along the length of the tubular portion 2. Preferably,the balloon 10 is compressed about the diameter of the tubular portion 2for insertion and withdrawal of the vascular sheath 1 into and out ofthe body.

Preferably, the balloon 10 is inflatable to different sizes to enableuse of the vascular sheath 1 in various procedures. For example, whenthe vascular sheath 1 is used in a procedure requiring repositioning thevascular sheath from a retrograde to an antegrade position in a bloodvessel, and vice versa, the balloon 10 is inflated so that it is smallerthan the inner diameter of the blood vessel and larger than thearteriotomy through which the vascular sheath 1 entered the bloodvessel. By sizing the balloon 10 larger than the arteriotomy throughwhich the vascular sheath 1 entered the blood vessel, the tubularportion 2 is prevented from completely exiting from the blood vesselduring manipulation from a retrograde to an antegrade position, and viceversa. The vascular sheath 1 can also be used to aspirate blood clots,emboli and other materials from the blood vessel. When used in this way,the balloon 10 is inflated until it obstructs the blood vessel. In sucha procedure, the vascular sheath 1 is inserted into the blood vesselwith the distal end 6 of the tubular portion 2 facing towards thematerial to be aspirated. If the material, for example, a blood clot,has lodged in the blood vessel, antegrade flow will apply a pressurehead to keep this clot lodged in its position. The balloon 10 is theninflated until it occludes the blood vessel, thereby blocking blood flowthrough the blood vessel. Back-bleeding will then cause the blood clotto propagate towards the vascular sheath 1. An aspiration deviceconnected to the side arm 14 of vascular sheath 1 can then be used toaspirate the blood clot out of the blood vessel through the lumen 3.Thus, the vascular sheath 1 could be inserted into the blood vessel in aretrograde position, the balloon inflated to occlude the blood vesseland blood clots, emboli and other materials could be aspirated from oneside of the blood vessel, followed by partial deflation of the balloon10, repositioning of the vascular sheath 1 to an antegrade position,re-inflation of the balloon 10 to occlude the blood vessel, andaspiration of and blood clots, emboli and other materials on the otherside of the blood vessel.

When the vascular sheath is used to aspirate materials out of the bloodvessel, it is preferable to form the vascular sheath 1 and balloon 10 ina manner that will prevent the emboli, blood clots and other materialsfrom being lodged between the balloon 10 and the distal end 6 of thetubular portion 2. For example, in one embodiment, the vascular sheath 1and balloon 10 are formed so that the balloon 10 is flush with thedistal end 6 of the tubular portion 2, as shown in FIGS. 3 and 5. Inanother embodiment, the vascular sheath 1 and balloon 10 are formed sothat the balloon 10 extends beyond the distal end 6 of the tubularportion 2. In yet another embodiment, the vascular sheath 1 and balloon10 are formed so that the balloon 10 extends behind the distal end 6 ofthe tubular portion 2. In one embodiment, as shown in FIG. 6, theballoon 10 is in the form of a round or oval shaped balloon that, wheninflated, expands flush with the distal end 6 of the tubular portion 10.In another embodiment, as shown in FIGS. 3 and 5, the balloon 10 isfunnel-like or cone-like in shape, wherein the large end of the funnelor cone is at the distal end 6 of the tubular portion 2 and inflatesperpendicular and flush with the distal end 6 of the tubular portion 2.The funnel can also protrude out in front of distal end 6, to create atrue “funnel” appearance of the balloon and distal tip. Still further,the funnel can also extend so that it is behind the front of distal end6. In another embodiment, the balloon 10 is U-like in shape, as shown inFIGS. 21 a-c. The U-shaped balloon 10 can protrude out in front of thedistal end 6 of the tubular portion 2, as shown on FIG. 21 a, can extendbehind the distal end 6 of the tubular portion 2, as shown on FIG. 21 bor can extend flush with the distal end 6 of the tubular portion 2, asshown on FIG. 21 c. These embodiments will provide complete aspirationof the emboli, blood clots and other materials from the blood vessel.

When the vascular sheath 1 is used to insert a stent or performangioplasty, the balloon 10 is also preferably inflated until itobstructs the vessel. A wire (not shown) is used to cross through theobstruction. Then the stent (not shown) is deployed or angioplastyperformed, thus opening the blood vessel. During the manipulation of thewire and stent, it is possible to withdraw blood, blood clots, anddebris by aspiration through side arm 14. Alternatively, the aspirationcan take place after the stent has been deployed. This would bedetermined by the location of the sheath relative to the lesion (i.e.upstream vs. downstream).

The size of the balloon 10 is not particularly limited. For example,when the device is used within a blood vessel, the inflated crosssection of the balloon 10, as measured perpendicular to the length ofthe tubular portion, can range from its deflated size to as large as, orlarger than, the inner diameter of the blood vessel. When used on otheranatomical structures, the inflated cross section of the balloon 10 mayvary and is limited only by the size of the anatomical structure and theparticular requirements of the procedure. Preferably, so that the devicecan be used for various procedures requiring various inflation sizes,the balloon 10 is inflatable to any size in between its deflated sizeand its maximum inflated size by simply controlling the amount of air ormaterial injected into the balloon 10. The length of the balloon, asmeasured parallel to the length of the tubular portion 2 is not limitedand, for example, when the device is used in blood vessels, ispreferably no greater than three quarters the length of the tubularportion 2, more preferably, between about 1 mm and about 150 mm, morepreferably, between about 3 mm and about 40 mm.

Inflation of the balloon 10 is accomplished through an inflation port12. In a preferred embodiment, as shown in FIGS. 7-10, the wall of thetubular portion, which extends from the inner diameter of the tubularportion to the outer diameter of the tubular portion, has embeddedinside one or more inflation channels 22 that connect the inflation port12 to the balloon 10. In a preferred embodiment, the balloon 10 ismounted over a portion of the distal end 6 of the tubular portion 2. Theone or more channels 22 extend from the balloon inflation port 12 to apoint on the tubular portion 2 covered by the balloon 10. One or moreapertures 30 are located along the length of the tubular portion 2covered by the balloon 10 such that air or other material insertedthrough inflation port 12 passes through the one or more channel 22,through the one or more apertures 30 and into the balloon 10.

In one embodiment, as shown in FIGS. 9 and 10, a single tubularinflation channel 22 connects the inflation port 12 to the balloon. Inthis embodiment, one or more apertures 30 may be located in the tubularportion 2 covered by the balloon 10 in the pathway of the inflationchannel 22. In another embodiment, as shown in FIG. 8, the wall of thetubular portion 2 can be hollow along its circumference between theinner diameter and the outer diameter of the tubular portion 2, and thechannel 22 comprises the hollow portion. As shown in FIG. 11, one ormore apertures 30 may be located along the circumference of the tubularportion 2 in the portion covered by the balloon 10. Alternatively, anopen circular strip 32 may be formed along the circumference of thetubular portion 2 covered by the balloon 10 for conveying the air orother balloon inflation materials from the channel 22 into the balloon10.

In another embodiment, as shown in FIG. 12, the mechanism that preventsthe device from pulling out of an anatomical structure during complexinterventions, e.g. when switching from an antegrade to a retrogradeapproach in a blood vessel and vice versa, comprises a plurality ofballoons 10 a located near the distal end 6 of the tubular portion 2.The plurality of balloons 10 a are preferably located about the outercircumference of the tubular portion 2. The fabrication and design ofthe plurality of balloons 10 a are similar to the fabrication and designof the single balloon 10 described above. For example, the materialsused on fabricating the plurality of balloons 10 a are the same as thoseused in fabricating the single balloon 10. The balloons 10 a arepreferably compressed to the diameter of the tubular portion 2 forinsertion and withdrawal of the vascular sheath 1. Further, the balloons10 a are preferably inflatable to different sizes to enable use of thedevice in various procedures. For example, when the device is used in ablood vessel, the balloons 10 a are preferably inflatable to a sizewherein the cross section of the tubular portion 2 plus balloons 10 a islarger than the arteriotomy and to a size wherein the balloons 10 aobstruct the blood vessel.

The balloons 10 a can also come in a variety of shapes. For example,each of the balloons 10 a may inflate to a circular or oval shape. Inanother embodiment, the plurality of balloons 10 a may inflate such thatthe plurality of balloons 10 a together form a ring about the distal end6 of the tubular portion 2. In some embodiments, the ring inflates flushwith the distal end 6 of the tubular portion 2. In another embodiment,the plurality of balloons 10 a inflate such that, when inflated, theplurality of balloons 10 a together form a funnel-like shape. In someembodiments, the funnel-like shape may inflate flush with the distal end6 of the tubular portion 2. In other embodiments, the funnel can alsoprotrude out in front of distal end 6, to create a true “funnel”appearance of the balloon and distal end of the tubular portion.

For the plurality of balloons 10 a, there may be a single inflation port12 in fluid communication with all of the balloons 10 a or multipleinflation ports 12 a in fluid communication each of the balloons 10 a.One or more inflation channels 22 a embedded inside the tubular portion2 preferably connect the inflation port(s) 12 a to the balloons 10 a. Inone embodiment, a single inflation channel 22 extends from an inflationport 22 and splits to extend to each of the balloons 10 a, as shown inFIG. 13. Alternatively, the single inflation channel 22 can extendtowards the balloons 10 a and extend within the circumference of thetubular portion 2 to each balloon 10 a as shown in FIG. 14. In anotherembodiment, a plurality of inflation ports 12 a and inflation channels22 a can be formed in the tubular portion 2, for example, each extendingto a separate balloon 10 a.

In another embodiment, as shown in FIGS. 15-18, the mechanism thatprevents the device from pulling out of an anatomical structure is inthe form of one or more extensions 11 near the distal end 6 of thetubular portion 2. For example, two or more arm-like extensions 11 canbe located near the distal end 6 of the tubular portion 2, as shown inFIG. 15. In another embodiment, one or more extensions 11 forming afunnel-like shape are located near the distal end 6 of the tubularportion 2, as shown in FIGS. 16 and 17. For example, as shown in FIG.16, a plurality of extensions 11 may deploy to connect together and forma funnel shape. In another embodiment, a plurality of extensions 11 maydeploy with a material 52 connecting the extensions 11 together, like anumbrella, to form a funnel shape, as shown in FIG. 17. Any type ofbiocompatible material may be used to connect the extensions. In yetanother embodiment, one or more extensions 11 forming a circular shapeare located near the distal end 6 of the tubular portion 2, as shown inFIG. 18. As with the funnel shape, the plurality of extensions 11 maydeploy to connect together and form a circular shape or, for example,the plurality of extensions 11 may deploy with a material 52 connectingthe extensions 11 together to form a circular shape.

These extensions 11 are preferably retractable to allow for retractionand deployment of the extensions 11 during use of the device. Adeployment/retraction mechanism (not shown) is preferably located nearthe proximal end of the device so that a user of the device can remotelyretract and deploy the extensions 11 during use. Preferably, theextensions 11 would be deployable by the user of the device such that,during insertion and withdrawal of the device into and out of theanatomical structure, the extensions 11 would be in their retractedstate and the cross section of the tubular portion 2 as the device isinserted and withdrawn is not increased or not significantly increasedby the extensions. For example, the extensions could be housed withinthe tubular portion 2 or, for example, folded back against the sidesurfaces of the tubular portion 2 during insertion of the device intothe anatomical structure. Upon insertion of the device into theanatomical structure to the desired site, the extensions 11 could thembe deployed by the user using the deployment/retraction mechanism. Priorto withdrawal of the device from the anatomical structure, theextensions 11 would be returned to their retracted state using thedeployment/retraction mechanism.

In some embodiments, the extensions 11 are deployable to different sizesto enable use of the devices in various procedures. For example, whenthe device is a vascular sheath used in a procedure requiringrepositioning the vascular sheath from a retrograde to an antegradeposition, and vice versa, the extensions 11 are deployed so that thecross section of the tubular portion 2 plus extensions 11 is smallerthan the inner diameter of the blood vessel and larger than thearteriotomy through which the vascular sheath 1 entered the bloodvessel. By sizing the extensions 11 so that the cross section of thetubular portion 2 plus extensions 11 is larger than the arteriotomythrough which the vascular sheath 1 entered the blood vessel, thetubular portion 2 is prevented from completely exiting from the bloodvessel during manipulation from a retrograde to an antegrade positionand vice versa.

In some embodiments, the vascular sheath 1 is used to aspirate bloodclots, emboli and other materials from the blood vessel. When used inthis way, the extensions 11 are designed such that when fully deployed,the blood vessel is obstructed. In such a procedure, the vascular sheath1 is inserted into the blood vessel with the distal end 6 of the tubularportion 2 facing towards the material to be aspirated. If the material,for example, a blood clot, has lodged in the blood vessel, antegradeflow will apply a pressure head to keep this clot lodged in itsposition. The extensions 11 are then deployed until they occlude theblood vessel, thereby blocking blood flow through the blood vessel.Back-bleeding will then cause the blood clot to propagate towards thevascular sheath 1. An aspiration device connected to the side arm 14 ofvascular sheath 1 can then be used to aspirate the blood clot out of theblood vessel through the lumen 3, or alternatively, a catheter can beplaced through the vascular sheath 1 and hemostatic valve 8 to thelocation of the obstruction and the material could be aspirated throughthe catheter. Thus, the vascular sheath 1 could be inserted into theblood vessel in a retrograde position, the extensions 11 deployed toocclude the blood vessel and blood clots, emboli and other materialscould be aspirated from one side of the blood vessel, followed bypartial deployment of the extensions 11, repositioning of the vascularsheath 1 to an antegrade position, re-deployment of the extensions 11 toocclude the blood vessel, and aspiration of and blood clots, emboli andother materials on the other side of the blood vessel.

When the vascular sheath 1 is used to insert a stent or performangioplasty, the extensions 11 are also preferably deployed until theyobstruct the vessel. A wire is used to cross through the obstruction.Then the stent is deployed or angioplasty performed, thus opening theblood vessel. During the manipulation of the wire and stent it ispossible to withdraw blood, blood clots, and debris by aspirationthrough side arm 14. Alternatively, the aspiration can take place afterthe stent has been deployed or using a Fogarty balloon to pull debrisout through the sheath. This would be determined by the location of thesheath relative to the lesion (i.e. upstream vs. downstream).

The size of the extensions 11 is not particularly limited. For example,when the device is used within a blood vessel, the deployed crosssection of the extensions 11, as measured perpendicular to the length ofthe tubular portion, can range from just larger than the incisionthrough which the tubular portion 2 was inserted into the blood vesselto as large as the inner diameter of the blood vessel. When used onother anatomical structures, the deployed cross section of theextensions 11 may vary and is limited only by the size of the anatomicalstructure and the particular requirements of the procedure. Preferably,so that the device can be used for various procedures requiring variousdeployment sizes, the extensions 11 are deployable to any size inbetween its retracted size and its maximum deployed size by simplycontrolling the amount of deployment and retraction of the extensions11.

A side-arm 14 in fluid communication with the lumen 3 may also belocated near the proximal end 4 of the tubular portion 2. The generalfeatures of the side-arm 14 are not particularly limited and may be inaccordance with side-arms of conventional vascular sheaths.

The side-arm 14 can be used to allow air, emboli, blood clots and othermaterials to be evacuated from the anatomical structure through thetubular portion 2 and to allow agents, such as medicaments,anticoagulants and contrast media to be injected into the tubularportion 2 if desired. A stopcock 28 or similar mechanism is preferablyattached to the end of the side arm 22 to selectively provide a seal.

When the side-arm 14 is used to aspirate emboli, blood clots and othermaterials from the anatomical structure, the side-arm 14 and stopcock 28preferably has an inner diameter at least as large as the lumen 3 of thetubular portion 2 so that materials aspirated through the tubularportion 2 fit through the side-arm 14 and do not become lodged at theopening of the side-arm 14.

In some embodiments, the device of the present invention could beinserted in a target blood vessel or anatomical structure, and alsoconnected to a recipient blood vessel or anatomical structure. Forexample, the device may be inserted into a blood vessel and alsoconnected to another blood vessel, usually a vein, by either a surgicalcutdown or using a percutaneous technique. This embodiment wouldeffectively create an arterial venous shunt/circuit. For example, in oneembodiment the tubular portion of the device is inserted in the targetanatomical structure and the side-arm 14 is connected to a recipientanatomical structure, thereby creating a continuous flow reversalcircuit from the target anatomical structure, through the distal end ofthe tubular portion, through the tubular portion, through the side arm,and into a target anatomical structure.

Such a continuous flow reversal circuit would require access to therecipient anatomical structure. For example, in some embodiments, theside arm 14 could be directly inserted in the recipient anatomicalstructure. In other embodiments, the side arm 14 or another portion ofthe device could be connected to tubing that is inserted in therecipient anatomical structure. In other embodiments, the device of thepresent invention is connected to a recipient anatomical structure via aconventional guide catheter or conventional vascular sheath. In otherembodiments, the side arm 14 or another portion of the device of thepresent invention is connected to a second device in accordance with thepresent invention such that the tubular portion of the first device isinserted in the target anatomical structure and the tubular portion ofthe second device is inserted into the recipient anatomical structure.The first and second devices are connected to each other, for example,via the side arms 14 of each device or, for example, via the hemostaticvalves 8 of each device through tubing connecting the two hemostaticvalves 8 together.

Such continuous flow reversal would be useful, for example, inperforming a procedure wherein materials, for example emboli, bloodclots, or blood, are transferred from a donor blood vessel into arecipient blood vessel. The device of the present invention could beused to occlude a donor vessel and prevent emboli, blood clots and othermaterials from propagating into the cerebral or cornary vasculature. Theemboli, blood clots and other materials could then be transferred to arecipient blood vessel wherein the danger of having the materialspropagate into the cerebral or coronary vasculature is eliminated. Inaddition to occluding the donor vessel, the mechanism would prevent thedevice from being pulled from the donor vessel during the transfer. Inthis embodiment, the device would be inserted in the donor blood vesseland, a continuous flow reversal could be created by forming a circuitbetween the “donor” vessel housing the embolic material to a “recipient”vessel elsewhere in the body. Vascular access to the recipient vesselwould then be provided, for example, via the side arm 14, a tube, aguide catheter, a vascular sheath or another device in accordance withthe present invention. In some embodiments, a pumping mechanism isinterposed in the circuit between the donor and recipient vessels toassist in reversing the blood flow.

Preferably, during the continuous flow reversal procedure, the balloon(s) 10 or extensions 11 could be retracted or partially retracted at anypoint in the procedure to allow reperfusion of blood flow through theblood vessel. Then, if desired, the transfer of materials from the donorto recipient blood vessel could be reestablished at any point simply byagain deploying the balloon(s) 10 or extensions 11 to occlude thevessel.

The continuous flow reversal described above could also be useful in aprocedure wherein blood is transferred from one patient to another orfrom one site to another in the same patient as in cardiac bypasssurgery. In such procedures, the device of the present invention, forexample, in the form of a vascular sheath or guide catheter, would beinserted into a donor patient's vessel. The device of the presentinvention would then be connected to a recipient patient's vessel via,for example, a tube, conventional guide catheter, conventional vascularsheath, or second device in accordance with the present invention. Thedevice of the present invention would be particularly helpful onpreventing the loss of vascular access during the blood transferprocedure.

While continuous flow reversal is described, in particular, wherein themechanism (e.g. balloon(s) 10 or extensions 11) are deployed to occludethe vessel, thereby preventing the flow of emboli, blood clots and othermaterials through the donor vessel, the mechanism could be retracted orpartially deployed so as to not occlude the vessel wherein the danger ofemboli, blood clots and other materials flowing through the donoranatomical structure is minimal. For example, in some embodiments, themechanism is only partially deployed so as to prevent the device fromlosing access to the anatomical structure.

The hemostatic valve 8 is located at the proximal end 4 of the tubularportion 2, as shown in the Figures. The general features of thehemostatic valve 8 are not particularly limited and may be in accordancewith hemostatic valves of conventional vascular sheaths.

The hemostatic valve 8 prevents leakage of blood and materials out ofthe anatomical structure through the device. In some embodiments, thehemostatic valve 8 can also be used to remove materials aspirated out ofthe anatomical structure. Preferably, when used to remove materialsaspirated out of the anatomical structure, the hemostatic valve 8 isremovably mounted on the proximal end 4 of the tubular portion 2 tofacilitate removal of materials out of the proximal end 4 of the tubularportion 2. Thus, the hemostatic valve 8 could be removed after insertionand positioning of the device and inflation of the balloon 10 ordeployment of extensions 11 and materials aspirated directly out of theproximal end 4 of the tubular portion 2. While the hemostatic valve 8may be permanently mounted on the proximal end 4 of the tubular portion2 and materials can be aspirated and removed through the hemostaticvalve 8, it is generally easier to remove these materials through theproximal end 4 of the tubular portion 2 after removal of the hemostaticvalve 8.

The hemostatic valve 8 can be removably or permanently mounted on theproximal end 4 of the tubular portion 2 with any conventional means suchas, for example, using various adhesives, forming the tubular portion 2and hemostatic valve 8 with threaded portions so that the hemostaticvalve could be screwed on and off of the tubular portion 2, and byforming the hemostatic valve 8 to permanently or removably snap onto thetubular portion 2.

In one embodiment, rather than a single mechanism at or near the distalend 6 of the tubular portion 2, the device may further include a secondmechanism at or near the proximal end 4 of the tubular portion 2. Inthis embodiment, both the proximal end 4 and the distal end 6 would beinserted into the anatomical structure. For example, the device may beinserted distal end 6 first into a blood vessel, followed by insertionof the proximal end 4 into the blood vessel. A portion of the devicebetween the two mechanisms would include one or more balloon inflationports 12, in the embodiment where the mechanism for preventing thedevice from pulling out of the anatomical structure comprises one ormore balloons 10. In embodiments where the mechanism for preventing thedevice from pulling out of the anatomical structure comprises one ormore extensions 11, one or more deployment/retraction mechanisms arelocated along the portion of the device between the two mechanisms. Theinflation port(s) 12 or deployment/retraction mechanism(s) would remainexternal to the blood vessel during use such that the mechanism forpreventing the device from pulling out of the anatomical structure(balloons 10 or extensions 11) could be inflated/deployed anddeflated/retracted at any point during the procedure. This type of anembodiment would be particularly suitable for use as a shunt. A typicalprocedure using such a device would include carotid endarectomy wherethe device would be inserted proximal and distal to the lesion to beoperated on. The balloons 10 would be inflated to obstruct flow throughthe native vessel and flow through the shunt, around the lesion to beoperated on and back into the native vessel, distal to the aformentionedlesion.

The use of the device of the present invention can be further understoodfrom the following discussion and with reference to FIGS. 1-19. Thefollowing discussion relates to a device in the form of a vascularsheath used in connection with a blood vessel. However, it is to beunderstood that other types of devices for performing percutaneous andsurgical interventions (e.g. guide catheters) may be used in a similarmanner on various anatomical structures of the body.

The vascular sheath is generally used by the following procedure: thevascular sheath is prepared with the mechanism not deployed, i.e. theballoon 10 empty and preferably compressed about the tubular portion 2or the extensions 11 retracted. An incision is made to provide access tothe target site. For example, an incision may be made in the patient'supper thigh and a needle passed through the incision into the commonfemoral artery. A wire is passed through the needle into the artery andthe needle removed, leaving the wire in place. The vascular sheath withdilator is inserted, distal end 6 first, over the wire into the bloodvessel in the upper thigh. The dilator is then removed, leaving thesheath in place, inside the blood vessel. The vascular sheath is thendirected to the target location. Preferably, the vascular sheath isinserted into the blood vessel in a retrograde position towards thepatient's head. Indicia 24 can be used to determine the depth ofinsertion of the vascular sheath. The balloon 10, balloons 10 a, orextensions 11 can then be inflated or deployed.

More specifically, techniques currently used for the insertion of smallangiographic catheters is preferably utilized to insert the vascularsheath 1 (e.g. the Seldinger technique). See the Journal of The AmericanMedical Association, Jan. 31, 1977, Volume 237.

If the surgeon wishes to aspirate blood clots, emboli or other materialsout of the blood vessel, the balloon(s) 10, 10 a or extensions are theninflated or deployed until the vessel is occluded. The vessel is knownto be occluded when contrast injected through side-arm 14 into tubularportion 2 into the blood vessel is stagnant. An aspiration device canthen be connected stopcock 28 on the side-arm 14 and the blood clots,emboli or other materials can be aspirated out of the blood vesselthrough the side-arm 14. In another embodiment, the blood clots, embolior other materials can be removed through the hemostatic valve 8 byusing a Fogarty balloon to pull the blood clots out of the blood vessel,into the sheath and out to the hemostatic valve 8. In anotherembodiment, the hemostatic valve 8 is removably mounted on the tubularportion 2. Thus, the hemostatic valve 8 is first removed from theproximal end 4 of the tubular portion 2 and the aspiration device isthen attached to the proximal end of the tubular portion 2, so that theblood clots, emboli or other materials can be removed through thetubular portion 2 out the proximal end 4 or blood clots, emboli andother material pulled out of the vessel through the sheath by means of aFogarty balloon. In another embodiment, the hemostatic valve 8 isremovably mounted on the tubular portion 2. Thus, the hemostatic valve 8is first removed from the proximal end 4 of the tubular portion 2. Then,a Fogarty balloon is used to pull clot out of the blood vessel throughthe tubular portion 2 out the proximal end 4 and the silicon pinch valve40 is used to occlude the sheath once the Fogarty balloon has beenremoved and allow the user to re-attach the hemostatic valve 8 orsilicone septum 46.

If the surgeon wishes to inject agents, such as medicaments,anticoagulants and contrast media, into the blood vessel through thevascular sheath, the surgeon simply opens stopcock 28 and inserts asyringe or similar injection mechanism into the entrance of the side-arm14 and injects the agent.

When using the vascular sheath to implant a stent in the blood vessel,the device functions as an embolic protection device. The balloon(s) 10,10 a or extensions 11 are typically inflated/deployed to occlude theblood vessel. A wire is passed through the lumen 3 of tubular portion 2and across the narrowed or occluded blood vessel. The stent is mountedon an angioplasty balloon and is then advanced over the wire through thelumen 3 of the tubular portion 2 and positioned at the narrowed oroccluded portion of the blood vessel. The location can be confirmed byinjecting contrast medial through stopcock 28 of side-arm 14 into lumen3 of the tubular portion 2 into the blood vessel. The stent is deployedby either using an inflation device to inflate the angioplasty balloonor by unsheathing a self-expanding stent. The surgeon can aspiratethrough stopcock 28 of side-arm 14 during this process in order toprevent distal emboli if the vascular sheath is upstream from theocclusion. Additionally, a tubing circuit can be created betweenconnected stopcock 28 on the side-arm 14 and another vascular sheathplaced in a recipient blood vessel, usually a vein. A pump would beinterposed in this circuit to aspirate the blood clots, emboli or othermaterials, during the procedure, out of the target blood vessel throughthe side-arm 14, through the tubing, and then into the recipient bloodvessel.(already stated above) Moreover, if it is necessary during theprocedure to re-establish blood flow, as may be the case during aprolonged coronary intervention, the vessel segment can have the debriscleared via aspiration, the balloon can be deflated to allowreperfusion, and then the balloon can be re-inflated to allowcontinuance of the procedure. Alternatively, if the vascular sheath isdownstream from the lesion, the surgeon can wait until the stent isdeployed to aspirate any embolic material that has been trapped byballoon(s) 10, 10 a or extensions 11.

If the surgeon wishes to reposition the vascular sheath from aretrograde to an antegrade position and vice versa, the surgeon simplyinflates or partially deflates the balloon 10 or deploys or partiallywithdraws the extensions 11 until the tubular portion plus balloon(s)10, 10 a or extensions 11 are sized smaller than the inner diameter ofthe blood vessel but larger than the opening through which the vascularsheath entered the blood vessel. As such, the balloon(s) 10, 10 a orextensions are sized to enable manipulation of the vascular sheath 1within the blood vessel while preventing loss of vascular access. Thesurgeon then pulls the vascular sheath back towards the opening throughwhich the vascular sheath entered the blood vessel, then upwards andpartially out of the opening if necessary, and back into the bloodvessel in the opposite position. Often the dilator and a guidwire willbe placed through the vascular sheath and into the blood vessel topermit the safe re-advancement of the sheath well into the artery.Because the tubular portion 2 plus inflated balloon(s) 10, 10 a orextensions 11 are larger than the opening through which the vascularsheath entered the blood vessel, they prevent the vascular sheath 1 fromexiting the blood vessel and, thus, allow the surgeon to accessantegrade and retrograde positions in the blood vessel in a singleprocedure through a single incision.

If the surgeon wished to use the device of the present invention for thetreatment of hemodialysis access grafts, only one sheath would berequired, as compared to the two sheaths that are currently used inconventional methods. Using the device of the present invention, thesurgeon would introduce the sheath with the dilator in place into thegraft using Seldinger technique towards the venous anastomosis. Theballoon(s) 10, 10 a or extensions 11 on the tubular portion 2 could beused to angioplasty any narrowing of the graft or blood vessels, andalso could used to push any clots out of the graft, into the arm vein.The surgeon then pulls the vascular sheath back towards the openingthrough which the vascular sheath entered the blood vessel, then upwardsand partially out of the opening if necessary, and back into the bloodvessel in the opposite position, towards the arterial anastomosis. Thevascular sheath could then be used for access towards the arterial limb.Additionally, the vascular sheath with dilator could be advanced overthe wire to the arterial anastomosis. The balloon(s) 10, 10 a would beinflated or the extensions 11 deployed and the vascular sheath pulledback towards the opening through which the vascular sheath entered theblood vessel, then upwards and partially out of the opening ifnecessary, and back into the blood vessel in the opposite position,towards the venous anastomosis. The balloon(s) 10, 10 a will then bere-inflated to the diameter of the graft or the extensions re-deployedto the diameter of the graft and the vascular sheath used to push anyclots out of the graft and into the vein.

If the surgeon wishes to transfer materials from a target or donoranatomical structure to a recipient anatomical structure, the device ofthe present invention could be used to create continuous flow reversal.For example, the device of the present invention could be used totransfer materials, such as blood, clots and embolic materials, from oneblood vessel in a patient to another vessel in a patient. For example,the continuous flow reversal could be used to transfer materials, suchas clots and embolic materials, from a target vessel where there is arisk that the materials will propagate to the cerebral or coronaryvasculature to a recipient vessel wherein this risk is eliminated.Alternatively, the device of the present invention could be used totransfer blood and other materials from a donor patient's blood vesselto a recipient patient's blood vessel.

In this embodiment, the method would further involve providing access tothe recipient anatomical structure. For example, the device of thepresent invention could be connected to tubing, to a conventional guidecatheter, to a conventional vascular sheath, or to a second device inaccordance with the present invention, which, in turn is inserted in therecipient anatomical structure. Still further, in some embodiments, theside arm 14 of the device could be directly inserted in the recipientanatomical structure.

During the continuous flow reversal, the mechanism may be deployed toocclude the vessel, for example, if there is a risk that clots andembolic material may propagate to the cerebral vasculature.Alternatively, the mechanism may be deployed not to occlude the vessel,but, rather, to maintain vascular access if, for example, there isminimal risk that clots and embolic material may propagate to thecerebral vasculature. If the mechanism is deployed to occlude thevessel, the method of continuous flow reversal may further includereperfusion of blood. For example, if reestablishment of the flow ofblood to the heart is desired for a period of time during the procedure,the mechanism may be retracted during the procedure so that the vesselis no longer occluded and blood flow is reestablished. After perfusionof the blood is reestablished for a desired period of time, themechanism may again be deployed to occlude the vessel. In someembodiments, during reperfusion, the circuit between the target bloodvessel and recipient blood vessel can be blocked so that reperfusion iscarried out while transfer of materials from the donor to recipientblood vessel is stopped. Then, after perfusion of the blood isreestablished for a desired period of time, the circuit may then beopened to continue transfer of materials from the donor to recipientblood vessel. During this time, the vessel may remain not occluded ormay again be occluded by redeployment of the mechanism.

Upon completion of the procedure, the balloon(s) 10, 10 a is deflated orthe extensions 11 withdrawn and the vascular sheath 1 removed from theblood vessel.

It will be appreciated that the vascular sheath 1 is usable for any typeof surgical procedure wherein a vascular sheath is needed to providecommunication of medical devices with a patient's blood vessel, bodyorgan, or body cavity.

The present invention also includes kits that comprise one or moredevice of the invention, preferably packaged in sterile condition. Kitsof the invention also may include various sized tubular portions 2,balloons 10, 10 a, extensions 11, side-arms 14, hemostatic valves 8,needles, dilators, etc. for use with the device, preferably packaged insterile condition, and/or written instructions for use of the device andother components of the kit.

All documents mentioned herein are incorporated by reference herein intheir entirety.

The foregoing description of the invention is merely illustrativethereof, and it is understood that variations and modifications can beeffected without departing from the scope or spirit of the invention asset forth in the following claims.

1. A device for use during vascular percutaneous interventions,comprising: a tubular portion, having a proximal end and a distal end,and a lumen extending from the proximal end to the distal end; and aretractable mechanism near the distal end of the tubular portion, themechanism providing an increased cross section of the tubular portionwhen deployed and no increase or substantially no increase in crosssection of the tubular portion when retracted; whereby the tubularportion is introduced into a vessel using either an antegrade or aretrograde approach and whereby the tubular portion can be repositionedwithin the vessel from an antegrade to a retrograde approach and from aretrograde to an antegrade approach without losing vascular access. 2.The device of claim 1, wherein the device is a vascular sheath.
 3. Thedevice of claim 1, wherein the device is a guide catheter.
 4. The deviceof claim 1, further comprising a hemostatic valve near the proximal endof the tubular portion.
 5. The device of claim 4, wherein the hemostaticvalve is removable.
 6. The device of claim 1, further comprising asilicone pinch valve near the proximal end of the tubular portion. 7.The device of claim 4, further comprising a silicone pinch valvepositioned between the hemostatic valve and the distal end of thetubular portion.
 8. The device of claim 1, wherein the distal end of thetubular portion is beveled or sharpened to assist in puncturing thevessel.
 9. The device of claim 1, further comprising a side-armextending from near the proximal end of the sheath.
 10. The device ofclaim 1, wherein the tubular portion has an outer diameter no greaterthan 45 mm.
 11. The device of claim 10, wherein the tubular portion hasan outer diameter ranging from about 1 mm to about 70 mm.
 12. The deviceof claim 11, wherein the tubular portion has an outer diameter rangingfrom about 1 mm to about 8 mm.
 13. The device of claim 1, wherein thetubular portion has a length ranging from about 5 cm to about 135 cm.14. The device of claim 1, wherein the lumen has a diameter of at leastabout 1 mm.
 15. The device of claim 14, wherein the lumen has a diameterranging from about 70 mm to about 1 mm.
 16. The device of claim 15,wherein the lumen has a diameter ranging from about 1 mm to about 8 mm.17. The device of claim 1, wherein the retractable mechanism comprisesat least one inflatable balloon.
 18. The device of claim 17, furthercomprising at least one balloon inflation port near the proximal end ofthe tubular portion for inflation of the at least one balloon.
 19. Thedevice of claim 18, further comprising at least one inflation channelconnecting the at least one balloon to the at least one ballooninflation port.
 20. The device of claim 19, wherein the at least oneinflation channel is located in the walls of the tubular portion. 21.The device of claim 20, wherein the walls of the tubular portion arehollow and the at least one inflation channel comprises the hollow ofthe walls of the tubular portion.
 22. The device of claim 19, furthercomprising at least one aperture in the walls of the tubular portion,wherein the at least one aperture connects the at least one inflationchannel to the at least one balloon.
 23. The device of claim 17, whereinthe mechanism comprises a single inflatable balloon and wherein theballoon, when inflated, is circular or oval in shape.
 24. The device ofclaim 23, wherein the balloon, when inflated, has a cross-sectionaldiameter of no greater than 70 mm.
 25. The device of claim 24, whereinthe balloon, when inflated, has a cross-sectional diameter ranging fromabout 2 mm to about 70 mm.
 26. The device of claim 25, wherein theballoon, when inflated, has a cross-sectional diameter ranging fromabout 3 mm to about 20 mm.
 27. The device of claim 23, wherein theballoon, when inflated, has a length of no greater than three-quartersthe length of the tubular portion.
 28. The device of claim 23, whereinthe balloon, when inflated, has a length ranging from about 1 mm toabout 150 mm.
 29. The device of claim 17, wherein the mechanismcomprises a plurality inflatable balloons and wherein the balloons, wheninflated, form a circular or oval shape.
 30. The device of claim 17,wherein the mechanism comprises one or more inflatable balloons that,when inflated, form a funnel shape.
 31. (canceled)
 32. The device ofclaim 30, wherein the largest width of the funnel shaped balloon, wheninflated, is no greater than 70 mm.
 33. The device of claim 30, whereinthe largest width of the funnel shaped balloon, when inflated, rangesfrom about 2 mm to about 60 mm.
 34. The device of claim 30, wherein thelargest width of the funnel shaped balloon, when inflated, ranges fromabout 2 mm to about 20 mm.
 35. The device of claim 17, wherein the oneor more balloons, when inflated, are flush with the distal end of thetubular portion.
 36. The device of claim 17, wherein the one or moreballoons, when inflated, protrude in front of the distal end of thetubular portion forming a funnel.
 37. The device of claim 17 wherein theone or more balloons is inflatable to various sizes.
 38. The device ofclaim 1, wherein the retractable mechanism comprises at least oneretractable extension.
 39. The device of claim 38, wherein the atretractable mechanism comprises two or more arm-like extensions.
 40. Thedevice of claim 38, wherein the retractable mechanism comprises one ormore extensions forming a funnel-like shape.
 41. The device of claim 40,further comprising biodegradable material connecting the extensionstogether to form the funnel-like shape.
 42. The device of claim 36,wherein the retractable mechanism comprises one or more extensionsforming a circular shape.
 43. The device of claim 42, further comprisingbiodegradable material connecting the extensions together to form thecircular shape.
 44. The device of claim 38, wherein the at least oneretractable extension is housed within the tubular portion whenretracted.
 45. The device of claim 38, wherein the at least oneretractable extension is folded back against the side surfaces of thetubular portion when retracted.
 46. The device of claim 38, wherein theat least one retractable extension is deployable and retractable tovarious sizes.
 47. A medical device kit, comprising one or more of thedevices of claim
 1. 48. The kit of claim 47, wherein the one or moredevices are packaged in sterile condition.
 49. A method for performing avascular percutaneous intervention comprising utilizing the device ofclaim
 1. 50. A method for performing a vascular percutaneousintervention comprising the steps of: (a) providing a device comprising:a tubular portion, having a proximal end and a distal end, and a lumenextending from the proximal end to the distal end; a retractablemechanism near the distal end of the tubular portion, the mechanismproviding an increased cross section of the tubular portion whendeployed and substantially no increase in cross section of the tubularportion when retracted; (b) inserting the tubular portion of the deviceinto a blood vessel distal end first with the retractable mechanismretracted; (c) deploying the retractable mechanism to a size larger thanthe opening through which the tubular portion entered the blood vessel;(d) performing the vascular percutaneous intervention; (e) retractingthe retractable mechanism; and (f) removing the device from the bloodvessel.
 51. The method of claim 50, wherein the device is inserted usinga retrograde approach, wherein the retractable mechanism is deployed toa size larger than the opening through which the tubular portion enteredthe blood vessel, and wherein the method further comprises the step of,after (d), repositioning the device to an antegrade approach, whereinthe deployed retractable mechanism prevents the tubular portion fromexiting the blood vessel.
 52. The method of claim 50, wherein theretractable mechanism comprises at least one inflatable balloon.
 53. Themethod of claim 50, wherein the retractable mechanism comprises at leastone retractable extension.
 54. The method of claim 50, wherein thedevice is in the form of a guide catheter.
 55. A method of repositioninga device within a blood vessel between a retrograde approach and anantegrade approach and vice-versa, comprising utilizing the deviceclaim
 1. 56. A method of repositioning a device within a blood vesselbetween a retrograde approach and an antegrade approach and vice-versa,comprising: (a) providing a device comprising: a tubular portion, havinga proximal end and a distal end, and a lumen extending from the proximalend to the distal end; a retractable mechanism near the distal end ofthe tubular portion, the mechanism providing an increased cross sectionof the tubular portion when deployed and substantially no increase incross section of the tubular portion when retracted; (b) inserting thetubular portion of the device into a blood vessel in one directiondistal end first with the mechanism retracted; (c) deploying themechanism to a size larger than the opening through which the tubularportion entered the blood vessel; (d) pulling the device back out of theblood vessel, while maintaining vascular access; (e) pushing the deviceback into the blood vessel in the opposite direction whereby thedeployed mechanism prevents the device from losing vascular assess. 57.A method for aspirating blood clots, emboli and other materials from ablood vessel comprising the steps of: (a) providing a device comprising:a tubular portion, having a proximal end and a distal end, and a lumenextending from the proximal end to the distal end; a retractablemechanism near the distal end of the tubular portion, the mechanismproviding an increased cross section of the tubular portion whendeployed and substantially no increase in cross section of the tubularportion when retracted; (b) inserting the tubular portion of the deviceinto the blood vessel distal end first facing towards the material to beaspirated with the retractable mechanism retracted; (c) deploying theretractable mechanism to a size that occludes the blood vessel; (d)removing blood clots, emboli and other materials from the blood vessel;(e) retracting the retractable mechanism; and (f) removing the devicefrom the blood vessel.
 58. The method of claim 57, wherein the step of(d) removing blood clots, emboli and other materials from the bloodvessel comprises aspirating the blood clots, emboli and other materialsfrom the blood vessel through the tubular portion
 59. The method ofclaim 57, wherein the step of (d) removing blood clots, emboli and othermaterials from the blood vessel comprises pulling the blood clots,emboli and other materials from the blood vessel through the tubularporting using another balloon catheter.
 60. The method of claim 57,further comprising the steps of, after (d) removing the blood clot,emboli and other materials from the blood vessel; partially retractingthe retractable mechanism to a size smaller than the blood vessel butlarger than the opening through which the tubular portion entered theblood vessel; pulling the device back out of the blood vessel, whilemaintaining vascular access, whereby the deployed mechanism prevents thedevice from losing vascular assess; pushing the device back into theblood vessel in the opposite direction; deploying the retractablemechanism to a size that occludes the blood vessel; and aspirating bloodclots, emboli and other materials from the opposite direction of theblood vessel.
 61. The method of claim 49, wherein the device is a guidecatheter.
 62. The method of claim 49, wherein the device is a vascularsheath.
 63. A method for performing a vascular percutaneous interventioncomprising the steps of: (a) providing a first device comprising: atubular portion, having a proximal end and a distal end, and a lumenextending from the proximal end to the distal end; a retractablemechanism near the distal end of the tubular portion, the mechanismproviding an increased cross section of the tubular portion whendeployed and substantially no increase in cross section of the tubularportion when retracted; (b) inserting the tubular portion of the firstdevice into a donor blood vessel distal end first with the retractablemechanism retracted; (c) deploying the retractable mechanism to a sizelarger than the opening through which the tubular portion entered theblood vessel; (d) connecting the first device to a recipient bloodvessel; and (e) transferring materials from the donor blood vessel,through the tubular portion of the first device, and into the recipientblood vessel.
 64. The method of claim 63 wherein the step of (d)connecting the first device to a recipient blood vessel comprises thestep of connecting the first device to a tube and inserting the tubeinto the recipient blood vessel.
 65. The method of claims 63 wherein thefirst device further comprises a side arm and the step of (d) connectingthe first device to a recipient blood vessel comprises the step ofinserting the side arm the recipient vessel.
 66. The method of claim 63further comprising the step of providing a second device comprising atubular portion, having a proximal end and a distal end, and a lumenextending from the proximal end to the distal end and wherein the stepof (d) connecting the first device to a recipient blood vessel comprisesthe step of inserting the second device into recipient vessel andconnecting the first device to the second device.
 67. The method ofclaim 63, further comprising the step of interposing a pump between thefirst device and the recipient blood vessel, wherein the pump assists inaspirating materials from the donor blood vessel and into the recipientblood vessel, or visa-versa.
 68. The method of claim any one of claim 64wherein the tube further includes a retractable mechanism, the mechanismproviding an increased cross section of the tube when deployed andsubstantially no increase in cross section of the tube retracted. 69.The method of claim 63, wherein the step of (c) deploying theretractable mechanism to a size larger than the opening through whichthe tubular portion entered the blood vessel comprises deploying themechanism to a size that occludes the blood vessel and stops the bloodflow through the blood vessel.
 70. The method of claim 69, furthercomprising the steps of: (f) optionally stopping the transfer ofmaterials from the donor blood vessel into the recipient blood vessel;(g) optionally aspirating emboli, debris and other materials out of therecipient blood vessel through the tubular portion; (h) at leastpartially retracting the retractable mechanism to re-establish bloodflow through the donor blood vessel; (i) deploying the retractablemechanism to a size larger than the opening through which the tubularportion entered the blood vessel and optionally to a size that stopsblood flow through the donor blood vessel; and (j) reestablishing thetransfer of materials from the donor blood vessel into the recipientblood vessel if the transfer has been stopped.
 71. The method of claim66, wherein the first and/or second device is a guide catheter.